The sodium iodide symporter: Its emerging relevance to clinical thyroidology

European Journal of Endocrinology

Volumn 138, Issue 4, 1998, Pages 374-375

  Spitzweg, Christine ^a   Heufelder, Armin E ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE EXPRESSION REGULATION; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; SHORT SURVEY; THYROID DISEASE; THYROID HORMONE RELEASE; THYROID HORMONE SYNTHESIS;

CARRIER PROTEINS; GENE EXPRESSION; HUMANS; MEMBRANE PROTEINS; MUTATION; SYMPORTERS; THYROID DISEASES; THYROID GLAND; THYROTROPIN;

EID: 0031957468     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1380374     Document Type: Short Survey

References (12)

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9. - symporter. Nature Genetics 1997 16 124-125.
10. Matsuda A & Kosugi S. A homozygous missense mutation of the sodium/iodide symporter gene causing iodide transport defect. Journal of Clinical Endocrinology and Metabolism 1997 82 3966-3971.
11. Pohlenz J, Rosenthal I, Weiss RE & Refetoff S. Hypothyroidism due to iodide trapping defect caused by mutations in the sodium/ iodide symporter (NIS) gene. Thyroid 1997 7 (Suppl 1) S-108.
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